FDA Device Intelligence
HomeCAREFUSION 2200, INC › Snowden-Pencer

Snowden-Pencer

CAREFUSION 2200, INC · Model 89-8740 · UDI-DI 10885403156830

FSS Prescription
1
510(k) clearances
118
Adverse events
0
Recalls
38
Facilities

Description

SNOWDEN-PENCER LIGHT SOURCE 300 WATT XENON

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.